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10Inhibition of energy metabolism by 2-methylacetoacetate and 2-methyl-3-hydroxybutyrate in cerebral cortex of developing rats, Journal of Inherited Metabolic Disease Identification of heteroxygotes for the defect of mitochondrial 3-ketoacyl-CoA thiolase causing 2-methyl-3-hydroxybutyric aciduria, Journal of Inherited Metabolic Disease ??-Ketothiolase deficiency: Two siblings with different clinical conditions, Journal of Inherited Metabolic Disease Propionyl-CoA carboxylase deficiency with overflow of metabolites of isoleucine catabolism at all levels, European Journal of Pediatrics Mitochondrial 2-methylacetoacetyl-CoA thiolase deficiency: An inborn error of isoleucine and ketone body metabolism, Journal of Inherited Metabolic Disease 3-Ketothiolase deficiency, European Journal of Pediatrics Beta-ketothiolase deficiency in a family confirmed by in vitro enzymatic assays in fibroblasts, European Journal of Pediatrics Deranged isoleucine metabolism during ketotic attacks in patients with methylmalonic acidaemia, Journal of Inherited Metabolic Disease Beta-Ketothiolase Deficiency Presenting with Metabolic Stroke After a Normal Newborn Screen in Two Individuals, JIMD Reports, Volume 39 Excretion of 2-methyl-3-oxovaleric acid in propionic acidemia, European Journal of Pediatrics